rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare kidney inflammation causing rapid loss of kidney function.
is a rare inherited disorder causing sun sensitivity and progressive nerve problems.
is a rare genetic condition affecting growth, development, and hormone signaling.
is an allergic reaction to peach proteins, causing symptoms after exposure.
is a common food allergy causing hives, swelling, or life-threatening anaphylaxis.
is a rare mitochondrial disorder affecting blood cells, pancreas, and other organs.
is a rare genetic syndrome affecting the chest, head size, and nails.
is a childhood stroke caused by blocked blood flow to the brain.
is a rare childhood stomach disorder with collagen buildup and inflammation.
is a rare liver cancer that develops in children and teens.
is a rare childhood form of multiple sclerosis affecting the brain.
is an autoimmune disease causing inflammation that can affect many organs.
is an eye disease causing high pressure and vision loss in children.
is an inherited eye disease that raises pressure and can harm vision.
is an autoimmune condition causing an overactive thyroid in children.
is a common head lice infestation that causes scalp itching.
is a body lice infestation that causes itchy skin and irritation.
is a psychiatric disorder involving persistent sexual interest in prepubescent children.
is a rare genetic condition causing continual, usually painless skin peeling.
is a rare inherited condition causing painless, continual shedding of skin.
is a rare inherited skin disorder causing recurrent, inflammatory peeling and fragility.
is an inherited condition causing peeling skin, white nails, and thickened skin.
is a rare genetic disorder causing severe developmental delays and seizures.
is a rare genetic disorder causing early seizures and severe developmental delays.